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Polydioxanone Sterilized Surgical Needled Suture - India CDSCO Medical Device Registration

Polydioxanone Sterilized Surgical Needled Suture is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2020/000136_f728d67a060917635c23afd0fa5024fc_cc65f00a0c16a30d0119635a7ddc892c. This device is marketed under the brand name Synthetic. The license holder is Futura Surgicare Pvt Ltd, and it is classified as Device Class Class C. The approving authority is Sub Zonal Bangalore.

This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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CDSCO Registered
Class Class C
Polydioxanone Sterilized Surgical Needled Suture
UID: MFG/MD/2020/000136_f728d67a060917635c23afd0fa5024fc_cc65f00a0c16a30d0119635a7ddc892c

Brand Name

Synthetic

Device Class

Class C

Approving Authority

Sub Zonal Bangalore

Product Information

Polydioxanone monofilament synthetic absorbable sutures are indicated for use in all types of soft tissue approximation, including use in pediatric cardiovascular tissue where growth is expected to occur, and ophthalmic surgery. Polydioxanone suture is not indicated in adult cardiovascular tissue, microsurgery and neural tissue. These sutures are particularly useful where the combination of an absorbable suture and extended wound support (Synthetic) is desirable

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